unnamed protein product [Homo sapiens]

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[Identification and 3D architecture analysis of the LIPC gene mutation in a pedigree with familial hypercholesterolemia-like phenotype]. [Zhonghua Xin Xue Guan Bing Za ...]
[Identification and 3D architecture analysis of the LIPC gene mutation in a pedigree with familial hypercholesterolemia-like phenotype].
Zhang H, Li FY, Hao Y, Wang XM, Zhang J, Ma YL, Zeng H, Lin J. Zhonghua Xin Xue Guan Bing Za Zhi. 2023 Jul 24; 51(7):716-721.
Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia. [Circulation. 2022]
Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia.
Dijk W, Di Filippo M, Kooijman S, van Eenige R, Rimbert A, Caillaud A, Thedrez A, Arnaud L, Pronk A, Garçon D, et al. Version 2. Circulation. 2022 Sep 6; 146(10):724-739. Epub 2022 Jul 28.
Functional Haplotype of LIPC Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies. [Genes (Basel). 2021]
Functional Haplotype of LIPC Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies.
Liao YH, Er LK, Wu S, Ko YL, Teng MS. Genes (Basel). 2021 Jan 22; 12(2). Epub 2021 Jan 22.

RefSeq genomic sequence
See the genomic reference sequence for the LIPC gene (NG_011465.2).
RefSeq protein
See the reference protein sequence for hepatic triacylglycerol lipase precursor (NP_000227.2).

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
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Protein